FDA applicant

Rehasense USA, Inc.

Romeoville, IL1 decision2026–20260 recalls

FDA records 1 decision for Rehasense USA, Inc. (Romeoville, IL) in 2026: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Rehasense USA, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

FIG. 1 — Rehasense USA, Inc. by year, 2026–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Rehasense USA, Inc.

Which product codes does it file in?

What has FDA decided for it lately?